DNA/RNA Synthesis
DNA/RNA Synthesis(DNA/RNA合成)
RNA synthesis, which is also called DNA transcription, is a highly selective process. Transcription by RNA polymerase II extends beyond RNA synthesis, towards a more active role in mRNA maturation, surveillance and export to the cytoplasm.
Single-strand breaks are repaired by DNA ligase using the complementary strand of the double helix as a template, with DNA ligase creating the final phosphodiester bond to fully repair the DNA.DNA ligases discriminate against substrates containing RNA strands or mismatched base pairs at positions near the ends of the nickedDNA. Bleomycin (BLM) exerts its genotoxicity by generating free radicals, whichattack C-4′ in the deoxyribose backbone of DNA, leading to opening of the ribose ring and strand breakage; it is an S-independentradiomimetic agent that causes double-strand breaks in DNA.
First strand cDNA is synthesized using random hexamer primers and M-MuLV Reverse Transcriptase (RNase H). Second strand cDNA synthesis is subsequently performed using DNA Polymerase I and RNase H. The remaining overhangs are converted into blunt ends using exonuclease/polymerase activity. After adenylation of the 3′ ends of DNA fragments, NEBNext Adaptor with hairpin loop structure is ligated to prepare the samples for hybridization. Cell cycle and DNA replication are the top two pathways regulated by BET bromodomain inhibition. Cycloheximide blocks the translation of mRNA to protein.
DNA/RNA Synthesis 相关产品(463)
- GC17131StreptozocinCAS: 18883-66-4纯度: >98.00% / 98.50% / >99.00%
Streptozocin 是一种有效的 DNA 甲基化抗生素,是一种天然存在的亚硝基酰胺,在实验模型中广泛用于产生糖尿病。
- GC18094Blasticidin S HClCAS: 3513-03-9纯度: >95.00% / >98.00% / >96.00% / >99.50%
Blasticidin S HCl是一种从灰色链霉菌中分离的核苷类抗生素。
- GC18640cis-9,10-Methyleneoctadecanoic Acid methyl esterCAS: 3971-54-8
A cyclopropane fatty acid methyl ester
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC17131 | Streptozocin | 18883-66-4 | >98.00% / 98.50% / >99.00% | |
Streptozocin 是一种有效的 DNA 甲基化抗生素,是一种天然存在的亚硝基酰胺,在实验模型中广泛用于产生糖尿病。 | ||||
| GC17186 | Acyclovir | 59277-89-3 | >99.00% | |
Acyclovir是一种强效的口服抗病毒药物。Acyclovir具有抗疱疹活性,对 HSV-1 和 HSV-2 的 IC 50 值分别为 0.85μM 和 0.86μM。Acyclovir诱导细胞周期紊乱和细胞凋亡。 | ||||
| GC17198 | Cycloheximide | 66-81-9 | >98.00% | |
环己酰亚胺是一种抗生素,它在翻译水平上抑制蛋白质合成,仅对真核细胞的细胞质(80s)核糖体起作用。 | ||||
| GC17231 | CRT0044876 | 6960-45-8 | >98.00% | |
A cell-permeable inhibitor of Ape-1 | ||||
| GC17232 | P005672 hydrochloride | 1035979-44-2 | - | |
P005672 hydrochloride是一种新型的窄谱四环素衍生物,用于治疗中度至重度炎性非结节性痤疮。 | ||||
| GC17278 | Adenine sulfate | 321-30-2 | - | |
A purine base | ||||
| GC17386 | YK-4-279 | 1037184-44-3 | >98.00% | |
YK-4-279 阻断 RNA Helicase A (RHA) 与 EWS-FLI1(致癌蛋白)的结合。 YK-4-279 诱导细胞凋亡并对各种癌细胞显示出抗增殖活性。 YK-4-279 有一个手性中心,它可以分成两种对映体。 YK-4-279可用于癌症研究。 | ||||
| GC17418 | AbK | 1253643-88-7 | >98.00% | |
AbK (H-L-Photo-lysine) 是一种含有二氮丙啶的赖氨酸氨基酸,是一种光交联剂。 | ||||
| GC17601 | TH287 | 1609960-30-6 | >98.00% | |
A selective MTH1 inhibitor | ||||
| GC17716 | Oxaliplatin | 61825-94-3 | >98.00% / >99.50% | |
奥沙利铂(Oxaliplatin)是一种用于治疗癌症的细胞毒性化疗药物。 | ||||
| GC17750 | Raltitrexed | 112887-68-0 | >98.50% / >98.00% | |
An inhibitor of thymidylate synthase | ||||
| GC17897 | Triapine (3-AP) | 143621-35-6 | - | |
核糖核苷酸还原酶抑制剂 | ||||
| GC18014 | Floxuridine | 50-91-9 | >99.50% | |
Floxuridine是一种抗代谢药物类抗癌药,是胸苷酸合酶的特异性抑制剂。 | ||||
| GC18094 | Blasticidin S HCl | 3513-03-9 | >95.00% / >98.00% / >96.00% / >99.50% | |
Blasticidin S HCl是一种从灰色链霉菌中分离的核苷类抗生素。 | ||||
| GC18186 | L67 | 325970-71-6 | >98.00% | |
A DNA ligase inhibitor | ||||
| GC18640 | cis-9,10-Methyleneoctadecanoic Acid methyl ester | 3971-54-8 | - | |
A cyclopropane fatty acid methyl ester | ||||
| GC18751 | Reticulol | 26246-41-3 | - | |
A cAMP phosphodiesterase and DNA topoisomerase I inhibitor | ||||
| GC18840 | Gilvocarcin V | 77879-90-4 | - | |
An antitumor antibiotic | ||||
| GC18853 | 4-isocyanato TEMPO | 88418-69-3 | - | |
A spin label for RNA | ||||
| GC19098 | CeMMEC1 | 440662-09-9 | >99.50% | |
A selective TAF1 bromodomain 2 inhibitor | ||||
| GC19099 | CeMMEC13 | 1790895-25-8 | >98.00% | |
A selective TAF1 bromodomain 2 inhibitor | ||||
| GC19110 | COH29 | 1190932-38-7 | >98.00% | |
COH29是一种强效的核糖核苷酸还原酶(RNR)抑制剂,对RNR的α和β亚基的IC 50 为16μM。 | ||||
| GC19238 | Madrasin | 374913-63-0 | >99.50% | |
A cell-permeant inhibitor of pre-mRNA splicing | ||||
| GC19263 | NKP-1339 | 197723-00-5 | >98.00% | |
A ruthenium complex with anticancer activity | ||||
